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acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
adverse drug reaction
alpha glucosidase
alpha-synuclein
anesthesia, general
anterior horn cell disease
aspartate aminotransferase
biologic markers
bionic reconstruction
brachial plexus injury
bradykinesia
calf hypertrophy
cardiomyopathy
children
chromosomal abnormality
complications
congestive heart failure
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
developmental retardation
disability, neurological
dystroglycanopathies
efficacy
Emery-Dreifuss muscular dystrophy
enzyme treatment
enzyme, defect
epidemiology of neurology
gene
gene mutation
gene therapy
genetic neurologic disorders
glycogen storage disease
Gowers maneuver
Guillain Barre syndrome
Guillain Barre syndrome, passive transfer of
hepatomegaly
history of neurology
hypotonia
immunology and the nervous system
L-dopa
Lewy body
life expectancy
lysosomal storage disease
lysosomes, abnoral
molecular genetics
mortality
motor neuron disease
motor system
MRI, abnormal
muscle biopsy
muscle transfer
muscle wasting, diffuse
muscle weakness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myopathy
myopathy, metabolic
myopathy, quadriceps
nerve transfer
neuroleptic, atypical
neurologic disease, diagnoses of
Parkinson disease
Parkinson disease, etiology of
Parkinson disease, nonmotor problems of
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Pompe's disease of glycogen storage
Pompe's disease, infantile
preclinical
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
quality of life
respirator
respiratory failure
respiratory tract infection
review article
rigidity
rippling muscle disease
safety
scoliosis
sinemet
SMN1 gene
spinal muscular atrophy
spinal muscular atrophy, classification
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
storage disease of CNS
survival motor neuron gene
synucleinopathy
systemic illness
toe walking
tongue, enlarged
treatment of neurologic disorder
tremor
weakness
weakness, progressive
weakness, proximal
web sites
Werdnig-Hoffman disease
Showing articles 3200 to 3223 of 3223 << Previous

Guillain-Barre Syndrome Need for Exact Diagnostic Criteris
NEJM 262:964, Osler,J.,et al, 1960

Diseases of the Basal Ganglia-Their Relation to Disorders of Movement
Lancet 1099, 1960, Nov., Denny-Brown,D., 1960

Clinical Picture in Creutzfeldt-Jakob Disease
Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Infectious Neuronitis (Guillain-Barre Syndrome) in Children
Neurol 9:533-539, Peterman,A.F.,et al, 1959

Polyneuritis in Children
Pediatrics 22:972-990, Low,N.L.,et al, 1958

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Neuro CPC of MGH
Congenital Vascular Malfor. of Spinal Cord, NEJM 258:949-954958., , 1958

Neuro CPC of MGH
Meningeal Gliomatosis, NEJM 259:688-6931958., , 1958

Neuro CPC of MGH
Cerebral Infarcts Due to Paradoxical Emboli, NEJM 258:338-3451958., , 1958

The Significance of Nonbacterial Thrombotic Endocarditis:An Autopsy & Clinical Study of 78 Cases
Ann Int Med 46:255, MacDonald,R.A.,et al, 1957

Neurologic Manifestations of Chronic Pulmonary Insufficiency
NEJM 257:579-590, Austen,F.K.,et al, 1957

Polyradiculitis (Landry-Guillain-Barre Syndrome)
BMJ 480, March1957., Jackson,R.,et al, 1957

An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia)
NEJM 255:57, Fisher,C.M., 1956

Neurologic Signs & Symptoms as Early Manifestations of SLE
Neurol 5:84, Siekert,R.,et al, 1955

Landry-Guillain-Barre Syndrome:Cardiovascular Complications Treatment with ACTH & Cortisone
BMJ 1504, 1954 Dec., Clarke,E.,et al, 1954

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

Ophthalmoplegia with Isolated Extraocular Muscle Hypertropny
JAMA Neurol 81:190-191, Li,C.M.F., et al,

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,



Showing articles 3200 to 3223 of 3223 << Previous